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Brief Title: Study to Describe the Management and the Use of Healthcare Resources in Patients With Chronic Lymphocytic Leukemia (CLL) Initiating Venetoclax in Routine Clinical Practice
Official Title: Post-Marketing Observational Study (PMOS) to Describe the Management and the Use of Healthcare Resources in Patients With Chronic Lymphocytic Leukemia (CLL) Initiating Venetoclax in Routine Clinical Practice (DEVOTE)
Study ID: NCT03310190
Brief Summary: A study to assess the real-life management and use of healthcare resources during the initiation of: * Venetoclax in combination with rituximab is indicated for the treatment of adult participants with chronic lymphocytic leukemia (CLL) who have received at least one prior therapy. * Venetoclax in participants with CLL with the deletion of the short arm of chromosome 17 (del\[17p\]) who have received at least 1 prior therapy or participants with CLL without del(17p) who have received at least 1 prior therapy and for whom there are no other available treatment options.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
University of Calgary /ID# 166416, Calgary, Alberta, Canada
Cross Cancer Institute /ID# 166417, Edmonton, Alberta, Canada
Jack Ady Cancer Centre /ID# 217491, Lethbridge, Alberta, Canada
CancerCare Manitoba /ID# 170751, Winnipeg, Manitoba, Canada
The Moncton Hospital /ID# 166043, Moncton, New Brunswick, Canada
QE II Health Sciences Centre /ID# 213548, Halifax, Nova Scotia, Canada
William Osler Health System /ID# 202049, Brampton, Ontario, Canada
Kingston Health Sciences Centre /ID# 169252, Kingston, Ontario, Canada
Ottawa Hospital Research Institute /ID# 166041, Ottawa, Ontario, Canada
Health Sciences North /ID# 205817, Sudbury, Ontario, Canada
Thunder Bay Regional Research Institute /ID# 204740, Thunder Bay, Ontario, Canada
Jewish General Hospital /ID# 166418, Montreal, Quebec, Canada
CISSSBSL -Hopital regional de Rimouski /ID# 201202, Rimouski, Quebec, Canada
Name: ABBVIE INC.
Affiliation: AbbVie
Role: STUDY_DIRECTOR